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P M Conneally

Showing results (101-110 of 186) with videos related to

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Journal of Medical Genetics|July 13, 2002
Linkage stratification and mutation analysis at the Parkin locus identifies mutation positive Parkinson's disease familiesW C Nichols, N Pankratz, S K Uniacke, et al.
Cytogenetics and Cell Genetics|January 1, 1992
Chromosome 21 genetic linkage data set based on the Venezuelan reference pedigreeJ L Haines, J A Trofatter, R E Tanzi, et al.
Chest|June 1, 1997
The presence of genetic anticipation suggests that the molecular basis of familial primary pulmonary hypertension may be trinucleotide repeat expansionJ E Loyd, B Slovis, J A Phillips, et al.
Clinical Genetics|December 1, 1983
Linkage analysis in von Willebrand diseaseM S Verp, R M Radvany, D Green, et al.
Nature Genetics|September 1, 1993
Charcot-Marie-Tooth neuropathy type 1B is associated with mutations of the myelin P0 geneK Hayasaka, M Himoro, W Sato, et al.
Neurology|May 12, 2004
Genes influencing Parkinson disease onset: replication of PARK3 and identification of novel lociN Pankratz, S K Uniacke, C A Halter, et al.
Cytogenetics and Cell Genetics|January 1, 1978
Linkage group I: a statistically significant locus order from family studiesD A Meyers, A D Merritt, P M Conneally, et al.
Annals of Neurology|May 1, 1995
Cognitive scores in carriers of Huntington's disease gene compared to noncarriersT Foroud, E Siemers, D Kleindorfer, et al.
American Journal of Medical Genetics|January 1, 1980
Evidence of genetic variation for alpha-N-acetyl-D-glucosaminidase in black and white populations: a new polymorphismJ M Vance, M A Pericak-Vance, R C Elston, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 1, 1986
DNA linkage analysis of X chromosome-linked chronic granulomatous diseaseR L Baehner, L M Kunkel, A P Monaco, et al.
Pageof 19

Showing results (101-110 of 186) with videos related to

Sort By:
Pageof 19
Journal of Medical Genetics|July 13, 2002
Linkage stratification and mutation analysis at the Parkin locus identifies mutation positive Parkinson's disease familiesW C Nichols, N Pankratz, S K Uniacke, et al.
Cytogenetics and Cell Genetics|January 1, 1992
Chromosome 21 genetic linkage data set based on the Venezuelan reference pedigreeJ L Haines, J A Trofatter, R E Tanzi, et al.
Chest|June 1, 1997
The presence of genetic anticipation suggests that the molecular basis of familial primary pulmonary hypertension may be trinucleotide repeat expansionJ E Loyd, B Slovis, J A Phillips, et al.
Clinical Genetics|December 1, 1983
Linkage analysis in von Willebrand diseaseM S Verp, R M Radvany, D Green, et al.
Nature Genetics|September 1, 1993
Charcot-Marie-Tooth neuropathy type 1B is associated with mutations of the myelin P0 geneK Hayasaka, M Himoro, W Sato, et al.
Neurology|May 12, 2004
Genes influencing Parkinson disease onset: replication of PARK3 and identification of novel lociN Pankratz, S K Uniacke, C A Halter, et al.
Cytogenetics and Cell Genetics|January 1, 1978
Linkage group I: a statistically significant locus order from family studiesD A Meyers, A D Merritt, P M Conneally, et al.
Annals of Neurology|May 1, 1995
Cognitive scores in carriers of Huntington's disease gene compared to noncarriersT Foroud, E Siemers, D Kleindorfer, et al.
American Journal of Medical Genetics|January 1, 1980
Evidence of genetic variation for alpha-N-acetyl-D-glucosaminidase in black and white populations: a new polymorphismJ M Vance, M A Pericak-Vance, R C Elston, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 1, 1986
DNA linkage analysis of X chromosome-linked chronic granulomatous diseaseR L Baehner, L M Kunkel, A P Monaco, et al.
Pageof 19